Canonical Allele Identifier: CA27080792

Gene: TGFBR3

Linked Data

• dbSNP Id: rs1035429420
• gnomAD v3: 1-91866875-G-A
• gnomAD v4: 1-91866875-G-A
• MyVariant Identifiers: chr1:g.92332432G>A (hg19) ; chr1:g.91866875G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91866875G>A , CM000663.2:g.91866875G>A	GRCh38
NC_000001.10:g.92332432G>A , CM000663.1:g.92332432G>A	GRCh37
NC_000001.9:g.92105020G>A	NCBI36
NG_027757.1:g.44128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000212355.9:c.-113-5231C>T MANE Select	ENSP00000212355.4:n.-113-5231C>T
ENST00000212355.8:c.-113-5231C>T	ENSP00000212355.4:n.-113-5231C>T
ENST00000370399.6:c.-113-5231C>T	ENSP00000359426.2:n.-113-5231C>T
ENST00000417833.2:c.-200-33C>T	ENSP00000395975.2:n.-200-33C>T
ENST00000465892.6:c.-113-5231C>T	ENSP00000432638.1:n.-113-5231C>T
ENST00000532540.5:c.-113-5231C>T	ENSP00000434994.1:n.-113-5231C>T
ENST00000533370.1:n.123-2596C>T
NM_001195683.1:c.-113-5231C>T	NP_001182612.1:n.-113-5231C>T
NM_001195684.1:c.-113-5231C>T	NP_001182613.1:n.-113-5231C>T
NM_003243.4:c.-113-5231C>T	NP_003234.2:n.-113-5231C>T
NR_036634.1:n.403-5231C>T
XM_006710867.1:c.-113-5231C>T	XP_006710930.1:n.-113-5231C>T
XM_006710867.2:c.-113-5231C>T	XP_006710930.1:n.-113-5231C>T
NM_003243.5:c.-113-5231C>T MANE Select	NP_003234.2:n.-113-5231C>T
NM_001195683.2:c.-113-5231C>T	NP_001182612.1:n.-113-5231C>T
NR_036634.2:n.275-5231C>T